Job Summary
A company is looking for an Oncology Research Specialist - Regulatory Affairs & Compliance.
Key Responsibilities
- Assist with clinical, regulatory, and business documentation for oncology research projects
- Participate in study project start-up activities and maintain compliance documentation
- Monitor clinical trial compliance and manage patient eligibility documentation
Required Qualifications, Training, and Education
- High School Diploma or GED required; bachelor's degree preferred in Health/Science
- Experience in a healthcare setting preferred, especially in cancer care or clinical research
- Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred
- Ability to work remotely and maintain compliance in documentation
- Proficiency in maintaining electronic data repositories and filing systems
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